Manish Mukherjee, Arunavo Chatterjee, Soumyadip Bhunia and Pradipta Purkayastha*,
{"title":"疏水链诱导的三维钙钛矿纳米晶体到金纳米团簇接枝二维薄片的转化,用于光诱导电子转移衬底配方","authors":"Manish Mukherjee, Arunavo Chatterjee, Soumyadip Bhunia and Pradipta Purkayastha*, ","doi":"10.1021/acs.jpclett.3c01886","DOIUrl":null,"url":null,"abstract":"<p >Considering the augmentation of new generation energy harvesting devices and applications of electron–hole separation therein, conversion of 3D cubic CsPbBr<sub>3</sub> perovskite nanocrystals into 2D-platelets through ligand–ligand hydrophobic interactions has been conceived here. Cationic surfactants with various chain length coated the gold nanoclusters (AuNCs) that interact with oleic acid (OA) and oleylamine (OAm) coated 3D CsPbBr<sub>3</sub> nanocrystals to disintegrate the crystallinity of the perovskites and reformation of AuNC-grafted 2D-platelets of unusually large size. The planar perovskite-derivatives act as an exciton donor to the embedded AuNCs through photoinduced electron transfer (PET). This process is controlled by the optimum surfactant chain length. Transient absorption spectroscopy shows that the fastest radical growth time (4 ps) was with the 14-carbon containing tail of the surfactant, followed by the 16-carbon (45 ps) and the 12-carbon (290 ps) ones. PET is administered by the energy gaps of the participating candidates that control the transition dynamics. Our findings can be a potential tool to develop metal nanocluster-based hybrid 2D perovskite-derived platelets for optoelectronic applications.</p>","PeriodicalId":62,"journal":{"name":"The Journal of Physical Chemistry Letters","volume":"14 36","pages":"8251–8260"},"PeriodicalIF":4.8000,"publicationDate":"2023-09-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Hydrophobic Chain-Induced Conversion of Three-Dimensional Perovskite Nanocrystals to Gold Nanocluster-Grafted Two-Dimensional Platelets for Photoinduced Electron Transfer Substrate Formulation\",\"authors\":\"Manish Mukherjee, Arunavo Chatterjee, Soumyadip Bhunia and Pradipta Purkayastha*, \",\"doi\":\"10.1021/acs.jpclett.3c01886\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Considering the augmentation of new generation energy harvesting devices and applications of electron–hole separation therein, conversion of 3D cubic CsPbBr<sub>3</sub> perovskite nanocrystals into 2D-platelets through ligand–ligand hydrophobic interactions has been conceived here. Cationic surfactants with various chain length coated the gold nanoclusters (AuNCs) that interact with oleic acid (OA) and oleylamine (OAm) coated 3D CsPbBr<sub>3</sub> nanocrystals to disintegrate the crystallinity of the perovskites and reformation of AuNC-grafted 2D-platelets of unusually large size. The planar perovskite-derivatives act as an exciton donor to the embedded AuNCs through photoinduced electron transfer (PET). This process is controlled by the optimum surfactant chain length. Transient absorption spectroscopy shows that the fastest radical growth time (4 ps) was with the 14-carbon containing tail of the surfactant, followed by the 16-carbon (45 ps) and the 12-carbon (290 ps) ones. PET is administered by the energy gaps of the participating candidates that control the transition dynamics. Our findings can be a potential tool to develop metal nanocluster-based hybrid 2D perovskite-derived platelets for optoelectronic applications.</p>\",\"PeriodicalId\":62,\"journal\":{\"name\":\"The Journal of Physical Chemistry Letters\",\"volume\":\"14 36\",\"pages\":\"8251–8260\"},\"PeriodicalIF\":4.8000,\"publicationDate\":\"2023-09-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Journal of Physical Chemistry Letters\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.jpclett.3c01886\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Physical Chemistry Letters","FirstCategoryId":"1","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.jpclett.3c01886","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Hydrophobic Chain-Induced Conversion of Three-Dimensional Perovskite Nanocrystals to Gold Nanocluster-Grafted Two-Dimensional Platelets for Photoinduced Electron Transfer Substrate Formulation
Considering the augmentation of new generation energy harvesting devices and applications of electron–hole separation therein, conversion of 3D cubic CsPbBr3 perovskite nanocrystals into 2D-platelets through ligand–ligand hydrophobic interactions has been conceived here. Cationic surfactants with various chain length coated the gold nanoclusters (AuNCs) that interact with oleic acid (OA) and oleylamine (OAm) coated 3D CsPbBr3 nanocrystals to disintegrate the crystallinity of the perovskites and reformation of AuNC-grafted 2D-platelets of unusually large size. The planar perovskite-derivatives act as an exciton donor to the embedded AuNCs through photoinduced electron transfer (PET). This process is controlled by the optimum surfactant chain length. Transient absorption spectroscopy shows that the fastest radical growth time (4 ps) was with the 14-carbon containing tail of the surfactant, followed by the 16-carbon (45 ps) and the 12-carbon (290 ps) ones. PET is administered by the energy gaps of the participating candidates that control the transition dynamics. Our findings can be a potential tool to develop metal nanocluster-based hybrid 2D perovskite-derived platelets for optoelectronic applications.
期刊介绍:
The Journal of Physical Chemistry (JPC) Letters is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, chemical physicists, physicists, material scientists, and engineers. An important criterion for acceptance is that the paper reports a significant scientific advance and/or physical insight such that rapid publication is essential. Two issues of JPC Letters are published each month.